ENST00000635540.2:c.*198A>C
|
ENSP00000489185.1:n.*198A>C
|
|
ENST00000399799.3:c.3563A>C
MANE Select
|
ENSP00000382697.1:p.Glu1188Ala
|
|
ENST00000399799.2:c.3563A>C
|
ENSP00000382697.1:p.Glu1188Ala
|
|
ENST00000584687.1:n.273A>C
|
|
|
ENST00000635540.1:c.*198A>C
|
ENSP00000489185.1:n.*198A>C
|
|
NM_005406.2:c.3563A>C
|
NP_005397.1:p.Glu1188Ala
|
|
XM_011526136.1:c.3641A>C
|
XP_011524438.1:p.Glu1214Ala
|
|
XM_011526137.1:c.2174A>C
|
XP_011524439.1:p.Glu725Ala
|
|
XM_011526137.3:c.2174A>C
|
XP_011524439.1:p.Glu725Ala
|
|
NM_005406.3:c.3563A>C
MANE Select
|
NP_005397.1:p.Glu1188Ala
|
|